Literature DB >> 16209514

Three-component, room temperature crotylation catalyzed by solid-supported Brønsted acid: enantioselective synthesis of homoallylic carbamates.

Darren J Lipomi1, James S Panek.   

Abstract

[reaction: see text] A heterogeneous, three-component crotylation of in situ generated N-acyl iminium ions has been developed. This reaction proceeds under ambient temperature in MeCN and is catalyzed by macroporous polystyrene-bound sulfonic acid (MP-TsOH). Workup is accomplished by filtration, upon which the catalyst is recoverable. A range of homoallylic amine equivalents have been prepared from the corresponding aldehydes, carbamates, and chiral (E)-crotylsilanes in a highly stereoselective manner.

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Year:  2005        PMID: 16209514     DOI: 10.1021/ol051885s

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Annulations of enantioenriched allenylsilanes with in situ generated iminium ions: stereoselective synthesis of diverse heterocycles.

Authors:  Ryan A Brawn; James S Panek
Journal:  Org Lett       Date:  2009-01-15       Impact factor: 6.005

2.  Synthesis of enantioenriched homopropargylic sulfonamides by a three component reaction of aldehydes, sulfonamides, and chiral allenylsilanes.

Authors:  Ryan A Brawn; James S Panek
Journal:  Org Lett       Date:  2009-10-01       Impact factor: 6.005

3.  Reaction discovery employing macrocycles: transannular cyclizations of macrocyclic bis-lactams.

Authors:  Chong Han; Sathish Rangarajan; Alicia C Voukides; Aaron B Beeler; Richard Johnson; John A Porco
Journal:  Org Lett       Date:  2009-01-15       Impact factor: 6.005

  3 in total

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